| Weight | 415.496 g/mol |
|---|---|
| Formula | C19H17N3O4S2 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
cephaloridine (50-59-9)
Ceporin · Cephalomycine · Cefaloridine
Score:
#242 in Microbiology
,
#846 in Biochemistry
,
#2268 in Biology
,
#2794 in Chemistry
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- Acute toxicity of cephaloridine, an antibiotic derived from cephalosporin C (Toxicology and Applied Pharmacology, 1966)
- Renal and hepatic necrosis after metabolic activation of 2-substituted furans and thiophenes, including furosemide and cephaloridine (Toxicology and Applied Pharmacology, 1977)
- Lipid peroxidation: A possible mechanism of cephaloridine-induced nephrotoxicity (Toxicology and Applied Pharmacology, 1983)
- Nephrotoxicity due to cephaloridine: a light- and electron-microscopic study in rabbits. (The Journal of Infectious Diseases, 1970)
- Role of organic anion transporter 1 (OAT1) in cephaloridine (CER)-induced nephrotoxicity. (Kidney International, 1999)
- Depletion of renal glutathione content and nephrotoxicity of cephaloridine in rabbits, rats, and mice (Toxicology and Applied Pharmacology, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ceporin
- Cephalomycine
- Cefaloridine
- Cephaloridin
-
SMILESC1C(=C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CS3)C(=O)[O-])C[N+]4=CC=CC=C4
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InChIKeyCZTQZXZIADLWOZ-UHFFFAOYSA-N
- Pubchem - cephaloridine
- Wikipedia - cephaloridine
Cephaloridine (or cefaloridine) is a first generation semisynthetic derivative of cephalosporin C. It is unique among cephalosporins in that it exists as a zwitterion.
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